Robinow or "fetal face syndrome" in a male infant with ambiguous genitalia and androgen receptor deficiency
- PMID: 2373109
- DOI: 10.1007/BF02034745
Robinow or "fetal face syndrome" in a male infant with ambiguous genitalia and androgen receptor deficiency
Abstract
Typical features of the "fetal face" or Robinow syndrome are reported in a male infant who presented with ambiguous genitalia and persistence of the Mullerian ducts. Histology of the testes was normal whereas endocrinological studies showed partial deficiency of androgen receptors.